Clinical Research Coordinator

at  Icon Group

ABOUT YOU:

We are seeking a driven and detail-oriented individual who can independently solve problems. With relevant research experience, you will have the ability to manage your workflow and build rapport with various stakeholders through strong effective communication.
We are open to considering a highly skilled medical oncology or haematology nurse or pharmacists, as training in clinical trials is provided OR applicants with a bachelor’s degree in relevant health sciences, pharmacy or allied health field with relevant research coordination experience.

ABOUT THE ROLE:

Permanent full-time opportunity to join our collaborative research team based at the Icon Cancer Centre, Wesley. This is an amazing chance to work in a high-volume oncology and haematology clinical trial unit, along with gaining experience in phase 1 oncology clinical trials and access to leading technology.

KEY RESPONSIBILITIES:

• Provide high level support to Icon Principal Investigators in the conduct and day to day management of clinical trials
• Manage and conduct the clinical trial portfolio including the trial coordination, recruitment, participant and team member education and communication
• Ensure that clinical research carried out within Icon is conducted in accordance with Good Clinical Practice, the NHMRC National Statement and Icon policies
• Contribute to the financial management of the business unit to ensure that trial participants are tracked and patient payment data is submitted in a timely fashion
• Communicate effectively with trial participants to ensure that trial related procedures are booked appropriately and compliance to attendance for trial visits is maintained
• Actively attend meetings with internal and external stakeholders